Dr. Huntley's
Diagnosis
Checklist
Have a symptom?
See what questions
a doctor would ask.
See what questions
a doctor would ask.
TREATMENTS &
RESEARCH
Search the
latest
treatment
information
here.
latest
treatment
information
here.
Symptom Checker » Cracked skin » Diarrhea
Cracked skin and Diarrhea and Mouth infections and Muscle symptoms and Rash and Swallowing symptoms
Cracked skin AND Diarrhea AND Mouth infections AND Muscle symptoms AND Rash AND Swallowing symptoms: 2 causes
Cracked skin OR Diarrhea OR Mouth infections OR Muscle symptoms OR Rash OR Swallowing symptoms: 3009 causes
2. 18p minus syndrome
3. 1q deletion
4. 1q terminal deletion
5. 2-Hydroxyglutaricaciduria
6. 2-hydroxyethyl methacrylate sensitization
7. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
8. 2p21 deletion syndrome
9. 2q deletion
10. 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency
11. 3 alpha methylcrotonyl-coa carboxylase 2 deficiency
12. 3 alpha methylglutaconicaciduria, type 3
13. 3-Hydroxyisobutyric aciduria
14. 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency
15. 3-methylcrotonyl-CoA carboxylase deficiency
16. 3-methylglutaconic aciduria, type 1
17. 3-methylglutaconic aciduria, type 4
18. 3C syndrome
19. 4-hydroxyphenylacetic aciduria
20. 47,XXX syndrome
21. 49,XXXXY syndrome
22. 4p16.3 deletion
23. ?-hydroxybutyric aciduria
24. ACAD9 deficiency
25. ACTH Deficiency
26. ACTH resistance
27. ADANE
28. ADULT syndrome
29. AIDS wasting syndrome
30. AIDS-Related Complex
31. ALL-Down syndrome
32. ARCA
33. ARTS syndrome
34. ATR-X syndrome
35. Abdominal Cancer
36. Abdominal abscess
37. Aberrant subclavian artery abnormality
38. Abetalipoproteinemia
39. Ablepharon macrostomia syndrome
40. Abnormalities, Radiation-Induced
41. Absence of septum pellucidum and septo-optic dysplasia
42. Absent corpus callosum - cataract - immunodeficiency
43. Acanthamoeba infection
44. Acanthamoeba infection of the central nervous system
45. Acanthocytosis
46. Acanthosis nigricans muscle cramps acral enlargement
47. Accidental Eye Injury
48. Aceruloplasminemia
49. Acetyl-coa acetyltransferase 2 deficiency
50. Achalasia
51. Achalasia, familial esophageal
52. Achalasia, primary
53. Achard syndrome
54. Achlorhydria
55. Achondroplasia
56. Achor-Smith syndrome
57. Acid phosphatase deficiency
58. Acid-Base Imbalance
59. Acidemia, isovaleric
60. Acidemia, methylmalonic
61. Acidemia, propionic
62. Acne
63. Acquired Aplastic Anemia
64. Acquired agranulocytosis
65. Acquired angioedema
66. Acquired angioedema, type 1
67. Acquired angioedema, type 2
68. Acrocallosal Syndrome (Schinzel Type)
69. Acrodermatitis
70. Acrodermatitis Enteropathica
71. Acrodynia
72. Acromegaly
73. Actinic keratosis
74. Acute Appendicitis
75. Acute Disseminated Encephalomyelitis
76. Acute Gastritis
77. Acute Renal Failure
78. Acute adult T-Cell leukemia
79. Acute biphenotypic leukemia
80. Acute infections
81. Acute intermittent porphyria
82. Acute kidney failure
83. Acute leukaemia of ambiguous lineage
84. Acute lymphoblastic leukemia
85. Acute lymphoblastic leukemia, adult
86. Acute megacaryoblastic leukemia
87. Acute myeloblastic leukemia type 1
88. Acute myeloblastic leukemia type 2
89. Acute myeloblastic leukemia type 3
90. Acute myeloblastic leukemia type 4
91. Acute myeloblastic leukemia type 5
92. Acute myeloblastic leukemia type 6
93. Acute myeloblastic leukemia type 7
94. Acute myelocytic leukemia
95. Acute myelofibrosis
96. Acute myeloid leukaemia and myelodysplastic syndromes related to alkylating agent
97. Acute myeloid leukaemia and myelodysplastic syndromes related to topoisomerase type II inhibitor
98. Acute myeloid leukaemia and myelodysplastic syndromes, therapy related
99. Acute myeloid leukemia
100. Acute myeloid leukemia, adult
101. Acute myelosclerosis
102. Acute panmyelosis
103. Acute posterior multifocal placoid pigment
104. Acute tin poisoning
105. Acute zinc toxicity
106. Adams Nance syndrome
107. Addiction
108. Addington disease
109. Addison's Disease
110. Addisonian crisis
111. Adducted thumb syndrome recessive form
112. Adducted thumbs Dundar type
113. Adenocarcinoid tumor
114. Adenocarcinoma, Bronchiolo-Alveolar
115. Adenocarcinoma, Follicular
116. Adenoid cystic carcinoma
117. Adenophorea Infections
118. Adenosarcoma of the uterus
119. Adenoviridae Infections
120. Adenovirus infection in immunocompromised patients
121. Adenoviruses
122. Adenylosuccinate lyase deficiency
123. Adrenal Cancer
124. Adrenal Cortex Diseases
125. Adrenal Cortex Neoplasms
126. Adrenal adenoma, familial
127. Adrenal disorders
128. Adrenal gland hyperfunction
129. Adrenal gland hypofunction
130. Adrenal hemorrhage, neonatal
131. Adrenal hyperplasia, congenital type 3
132. Adrenal incidentaloma
133. Adrenal insufficiency
134. Adrenal medulla neoplasm
135. Adrenocortical carcinoma
136. Adrenoleukodystrophy
137. Adrenoleukodystrophy, autosomal, neonatal form
138. Adult Panic-Anxiety Syndrome
139. Adult SMA
140. Adult T-Cell leukemia
141. Adult T-cell leukemia/lymphoma
142. Adult onset Still's disease
143. Adult progressive spinal muscular atrophy, Aran Duchenne type
144. Adult-onset ALD
145. Adverse reaction
146. African Sleeping sickness
147. Agammaglobulinemia, alymphocytotic type
148. Agenesis of the corpus callosum
149. Aggressive NK-cell leukaemia
150. Aging brain syndrome
151. Agnathia-holoprosencephaly-situs inversus
152. Agyria-pachygyria type 1
153. Aicardi syndrome
154. Aicardi-Goutieres syndrome 1
155. Aicardi-Goutieres syndrome 2
156. Aicardi-Goutieres syndrome 3
157. Aicardi-Goutieres syndrome 4
158. Aicardi-Goutieres syndrome 5
159. Akesson syndrome
160. Al Gazali Sabrinathan Nair syndrome
161. Albright like syndrome
162. Albright's hereditary osteodystrophy
163. Alcohol Withdrawal
164. Alcohol-Induced Disorders
165. Alcohol-induced pseudo-Cushing syndrome
166. Alcoholic Neuropathy
167. Alcoholic intoxication
168. Alcoholic, reversible acute muscular
169. Alcoholism
170. Aldehyde syndrome
171. Aldolase A deficiency
172. Alexander Syndrome
173. Alkalosis
174. Allan-Herndon-Dudley Syndrome
175. Allen-Masters syndrome
176. Allergic Disorders
177. Allergic encephalomyelitis
178. Allergic reaction
179. Allergic rhinitis
180. Allergies
181. Allopurinol hypersensitivity syndrome
182. Alopecia mental retardation syndrome
183. Alopecia, epilepsy, oligophrenia syndrome of Moynahan
184. Alopecia, epilepsy, pyorrhea, mental subnormality
185. Alpers Syndrome
186. Alpha 1-Antitrypsin Deficiency
187. Alpha-N-acetylgalactosaminidase deficiency, Type III
188. Alpha-ketoglutarate dehydrogenase deficiency
189. Alport Syndrome
190. Altamira syndrome
191. Alternating hemiplegia of childhood
192. Aluminium toxicity
193. Alveolar Hydatid Disease
194. Alveolitis, extrinsic allergic
195. Alzheimer disease 10
196. Alzheimer disease 12
197. Alzheimer disease 13
198. Alzheimer disease 14
199. Alzheimer disease 15
200. Alzheimer disease 5
201. Alzheimer disease 6
202. Alzheimer disease 7
203. Alzheimer disease 8
204. Alzheimer disease 9
205. Alzheimer disease type 1
206. Alzheimer disease type 4
207. Alzheimer disease, familial
208. Alzheimer disease, familial, 1
209. Alzheimer disease, familial, type 3
210. Alzheimer's Disease
211. Alzheimer's disease without Neurofibrillary tangles
212. Amebiasis
213. Aminoacylase 1 deficiency
214. Amnesic shellfish poisoning
215. Amoebiasis
216. Amphetamine abuse
217. Amphetamine withdrawal
218. Ampola syndrome
219. Amyloid Neuropathies
220. Amyloid angiopathy
221. Amyloid cardiopathy
222. Amyloid cardiopathy, familial
223. Amyloidosis
224. Amyloidosis AL
225. Amyloidosis VII
226. Amyloidosis beta2-microglobulinic
227. Amyloidosis, familial cutaneous
228. Amyloidosis, inflammatory
229. Amyloidosis, oculoleptomeningeal
230. Amyopathic dermatomyositis
231. Amyotonia congenita
232. Amyotrophic lateral sclerosis
233. Amyotrophic lateral sclerosis 3
234. Amyotrophic lateral sclerosis 4, juvenile
235. Amyotrophic lateral sclerosis 5
236. Amyotrophic lateral sclerosis 6
237. Amyotrophic lateral sclerosis 7
238. Amyotrophic lateral sclerosis 8
239. Amyotrophic lateral sclerosis, 9
240. Amyotrophic lateral sclerosis, familial type 1
241. Amyotrophic lateral sclerosis, familial type 2
242. Amyotrophic lateral sclerosis, familial type 3
243. Amyotrophic lateral sclerosis, familial type 4
244. Amyotrophic lateral sclerosis, familial type 5
245. Amyotrophic lateral sclerosis, familial type 6
246. Amyotrophic lateral sclerosis, familial type 7
247. Amyotrophic lateral sclerosis, familial type 8
248. Analgesic nephropathy syndrome
249. Anaphylaxis
250. Ancylostoma duodenale
251. Andersen disease
252. Andrade's syndrome
253. Andropause
254. Anemia
255. Anemia, Sideroblastic
256. Anemia, hypochromic microcytic
257. Aneurysm, intracranial berry
258. Aneurysm, intracranial berry, 1
259. Aneurysm, intracranial berry, 2
260. Aneurysm, intracranial berry, 3
261. Aneurysm, intracranial berry, 4
262. Aneurysm, intracranial berry, 5
263. Aneurysm, intracranial berry, 6
264. Aneurysm, intracranial berry, 7
265. Aneurysm, intracranial berry, 8
266. Aneurysmal subarachnoid haemorrhage
267. Angelman syndrome
268. Angiofollicular ganglionic hyperplasia
269. Angioimmunoblastic T-cell lymphoma
270. Angioimmunoblastic with dysproteinemia lymphadenopathy
271. Angiokeratoma
272. Angioma hereditary neurocutaneous
273. Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert
274. Angiosarcoma of the liver
275. Angiostrongyliasis
276. Anguillulosis
277. Aniridia
278. Aniridia cerebellar ataxia mental deficiency
279. Ankylosing spondylarthritis
280. Ankylosis
281. Anorexia Nervosa
282. Anoxia
283. Ansell-Bywaters-Elderking syndrome
284. Anterior pituitary hyperhormonotrophic syndrome
285. Anthrax
286. Antimony poisoning
287. Antisynthetase syndrome
288. Anxiety
289. Anxiety Disorders
290. Anxiety-tension syndrome
291. Aortic Valve Insufficiency
292. Aortic arch anomaly with peculiar facies and mental retardation
293. Aortic arches defect
294. Aortic supravalvular stenosis
295. Appian-Plutarch syndrome
296. Aquagenous Urticaria
297. Arachnidism
298. Arachnoid Cysts
299. Arachnoiditis
300. Arakawa's syndrome 2
301. Arbovirosis
302. Arenavirus
303. Argentinean hemorrhagic fever
304. Arginase deficiency
305. Argininosuccinase lyase deficiency, late onset
306. Argininosuccinic aciduria
307. Arima syndrome
308. Arnold Stickler Bourne syndrome
309. Arnold-Chiari malformation type 3
310. Arnold-Chiari malformation type 4
311. Aromatic amino acid decarboxylase deficiency
312. Arsenic poisoning
313. Arteriosclerosis Obliterans
314. Arteriovenous Malformation
315. Arteritis
316. Arthritis
317. Arthrogryposis
318. Arthrogryposis due to muscular dystrophy
319. Arthrogryposis multiplex congenita, distal, X-linked
320. Arthrogryposis, distal, type 2A
321. Arthrogryposis-like disorder
322. Arthropathy, progressive pseudorheumatoid, of childhood
323. Asherson syndrome
324. Aspartylglycosaminuria
325. Asphyxia neonatorum
326. Asthma, Exercise-Induced
327. Astrovirus
328. Asymmetric septal hypertrophy
329. Ataxia
330. Ataxia Telangiectasia
331. Ataxia deafness reardon type
332. Ataxia spastic congenital miosis
333. Ataxia tapetoretinal degeneration
334. Ataxia with Vitamin E Deficiency
335. Ataxia with fasciculations
336. Ataxia, Hereditary, Autosomal Dominant
337. Ataxia, spastic, 3, autosomal recessive
338. Ataxia-deafness syndrome
339. Ataxia-oculomotor apraxia syndrome
340. Athabaskan brainstem dysgenesis
341. Athabaskan severe combined immunodeficiency
342. Athlete's foot
343. Ativan withdrawal
344. Atrial myxoma, familial
345. Attenuated familial polyposis
346. Atypical hemolytic uremic syndrome
347. Auriculo-condylar syndrome
348. Austrian syndrome
349. Autoimmune Hepatitis
350. Autoimmune Lymphoproliferative Syndrome
351. Autoimmune Myocarditis
352. Autoimmune Thrombocytopenia
353. Autoimmune Vasculitis
354. Autoimmune diseases
355. Autoimmune enteropathy
356. Autoimmune peripheral neuropathy
357. Autoimmune progesterone dermatitis
358. Autoimmune thyroid diseases
359. Autonomic Dysreflexia
360. Autonomic neuropathy
361. Avascular necrosis
362. Azotemia, famial
363. BANF acoustic neurinoma
364. Baber's syndrome
365. Babesiosis
366. Back tumour
367. Bacterial digestive infections
368. Bacterial endocarditis
369. Bacterial meningitis
370. Bacterial toxic-shock syndrome
371. Bahemuka Brown syndrome
372. Balance disorders
373. Balantidiasis
374. Balo disease
375. Balo's concentric sclerosis
376. Bangstad syndrome
377. Bannayan-Zonana syndrome
378. Banti's syndrome
379. Baraitser Brett Piesowicz syndrome
380. Baraitser burn fixen syndrome
381. Baraitser-Rodeck-Garner syndrome
382. Barakat syndrome
383. Barber's rash
384. Barbiturate abuse
385. Bard-Pic syndrome
386. Bare lymphocyte syndrome
387. Barmah Forest virus
388. Barotrauma
389. Barrett syndrome
390. Bartonella
391. Bartonella infections
392. Bartonellosis due to Bartonella quintana infection
393. Bartter's syndrome, antenatal type 1
394. Bartters syndrome, antenatal , type 2
395. Basal cell carcinomas with milia and coarse, sparse hair
396. Basal ganglia calcification, idiopathic 1
397. Basal ganglia disease, biotin-responsive
398. Basilar impression primary
399. Batten-Turner muscular dystrophy
400. Baughman syndrome
401. Bd syndrome
402. Beau's syndrome
403. Becker Muscular Dystrophy
404. Beckwith-Wiedemann Syndrome
405. Beer-drinker syndrome
406. Behcet's Disease
407. Bejel
408. Bell mania
409. Benign Paroxysmal Positional Vertigo
410. Benign familial infantile seizures 1
411. Benign familial neonatal-infantile seizures
412. Benign mucosal pemphigoid
413. Bentham-Driessen-Hanveld syndrome
414. Benzodiazepine abuse
415. Berardinelli-Seip congenital lipodystrophy
416. Berardinelli-Seip congenital lipodystrophy, type 1
417. Berardinelli-Seip congenital lipodystrophy, type 2
418. Bergman syndrome
419. Beriberi
420. Bernheim's syndrome
421. Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification
422. Berylliosis
423. Besnier-Boeck-Schaumann disease
424. Beta ketothiolase deficiency
425. Beta-ureidopropionase deficiency
426. Bethlem myopathy
427. Bhaskar-Jagannathan syndrome
428. Biliary Atresia
429. Biliary tract cancer
430. Bing-Neel syndrome
431. Binswanger's Disease
432. Biotin deficiency
433. Biotinidase deficiency
434. Birth Injury
435. Bland-Garland-White syndrome
436. Blast crisis
437. Blastocystis hominis
438. Blastomycosis
439. Blind loop syndrome
440. Blood cancer
441. Blood conditions
442. Blue and bloated syndrome
443. Bolivian hemorrhagic fever
444. Bone cancer
445. Bone-Marrow failure syndromes
446. Borjeson-Forssman-Lehmann Syndrome
447. Bornholm disease
448. Boron overuse
449. Borreliosis
450. Bortonneuse fever
451. Botulism food poisoning
452. Boudhina-Yedes-Khiari syndrome
453. Bovine spongiform encephalopathy
454. Bowel bypass syndrome
455. Bowel conditions
456. Bowel-associated dermatosis-arthritis syndrome
457. Brachycephalofrontonasal dysplasia
458. Brain cancer
459. Brain tumor, adult
460. Brainerd diarrhea
461. Branchio-skeleto-genital syndrome
462. Breast Duct Papilloma
463. Brennemann's syndrome
464. Bright's Disease
465. Brill disease
466. Bronchiolitis
467. Bronchopulmonary dysplasia
468. Brown-Symmers disease
469. Brown-Vialetto-Van Laere syndrome
470. Brucellosis
471. Brugada Syndrome
472. Bruyn-Scheltens syndrome
473. Bulimia nervosa
474. Bullous Pemphigoid
475. Burnout syndrome
476. Busulfan toxicity syndrome
477. CAMFAK syndrome
478. CDG syndrome (generic term)
479. COFS syndrome
480. Cadmium poisoning
481. Calcification of basal ganglia with or without hypocalcemia
482. Calciphylaxis
483. Camera-Marugo-Cohen syndrome
484. Campylobacter food poisoning
485. Campylobacter jejuni
486. Camurat-Engelmann disease, type 2
487. Camurati-Engelmann Disease
488. Canavan leukodystrophy
489. Cancer
490. Candidiasis
491. Carbamate insecticide poisoning
492. Carbamoyl-phosphate synthase 1 deficiency
493. Carbohydrate deficiency glycoprotein syndrome type II
494. Carbon monoxide poisoning
495. Carcinoid
496. Carcinoid syndrome
497. Carcinoma, squamous cell of head and neck
498. Cardiac malformation
499. Cardiac valvular dysplasia, X-linked
500. Cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency
501. Cardiofaciocutaneous Syndrome
502. Cardiomyopathy
503. Cardiomyopathy dilated 10
504. Cardiomyopathy dilated 1B
505. Cardiomyopathy dilated 1C
506. Cardiomyopathy dilated 1D
507. Cardiomyopathy dilated 1G
508. Cardiomyopathy dilated 1H
509. Cardiomyopathy dilated 1I
510. Cardiomyopathy dilated 1J
511. Cardiomyopathy dilated 1K
512. Cardiomyopathy dilated 1L
513. Cardiomyopathy dilated 1M
514. Cardiomyopathy dilated 1N
515. Cardiomyopathy dilated 1P
516. Cardiomyopathy dilated 1Q
517. Cardiomyopathy dilated 1R
518. Cardiomyopathy dilated 1S
519. Cardiomyopathy dilated 1T
520. Cardiomyopathy dilated 1U
521. Cardiomyopathy dilated 1W
522. Cardiomyopathy dilated 1Y
523. Cardiomyopathy dilated 1Z
524. Cardiomyopathy dilated with conduction defect
525. Cardiomyopathy dilated with conduction defect type 1
526. Cardiomyopathy dilated with conduction defect type 2
527. Cardiomyopathy due to anthracyclines
528. Cardiomyopathy with myopathy due to COX deficency
529. Cardiomyopathy, Alcoholic
530. Cardiospasm
531. Carnitine overuse
532. Carnitine palmitoyl transferase 1 deficiency
533. Carnitine palmitoyl transferase 2 deficiency
534. Carnitine palmitoyl transferase II deficiency, infantile hepatocardiomuscular type
535. Carnitine palmitoyl transferase II deficiency, lethal neonatal form
536. Carnitine palmitoyl transferase II deficiency, myopathic
537. Carnitine palmitoyl transferase deficiency
538. Carnitine transporter deficiency
539. Carnitine-acylcarnitine translocase deficiency
540. Cat scratch disease
541. Catalepsy
542. Cataract and cardiomyopathy
543. Cataract and congenital ichthyosis
544. Catastrophic Antiphospholipid Syndrome
545. Catatonia
546. Catatonic syndrome
547. Celiac Disease
548. Celiac disease, susceptibility to 1
549. Celiac disease, susceptibility to 10
550. Celiac disease, susceptibility to 11
551. Celiac disease, susceptibility to 12
552. Celiac disease, susceptibility to 13
553. Celiac disease, susceptibility to 2
554. Celiac disease, susceptibility to 3
555. Celiac disease, susceptibility to 4
556. Celiac disease, susceptibility to 5
557. Celiac disease, susceptibility to 6
558. Celiac disease, susceptibility to 7
559. Celiac disease, susceptibility to 8
560. Celiac disease, susceptibility to 9
561. Cellulitis
562. Central nervous system lymphoma, primary
563. Central nervous system oxygen toxicity
564. Central pontine myelinolysis
565. Central sleep apnea
566. Cephalothoracic progressive lipodystrophy
567. Cercarial dermatitis
568. Cerebellar abscess
569. Cerebellar agenesis
570. Cerebellar ataxia type 1, autosomal recessive
571. Cerebellar ataxia, X-linked
572. Cerebellar ataxia, dominant pure
573. Cerebellar ataxia, infantile with progressive external ophthalmoplegia
574. Cerebellar atrophy with progressive microcephaly
575. Cerebellar degeneration, subacute
576. Cerebellar hypoplasia
577. Cerebelloparenchymal autosomal recessive disorder 3
578. Cerebelloparenchymal disorder V
579. Cerebral Amyloid Angiopathy, Familial
580. Cerebral Atrophy
581. Cerebral Palsy
582. Cerebral abscess
583. Cerebral astrocytoma, adult
584. Cerebral cavernous malformations
585. Cerebral hemorrhage
586. Cerebral palsy, spastic, diplegic
587. Cerebral ventricle neoplasm
588. Cerebro oculo skeleto renal syndrome
589. Cerebrorenodigital syndrome
590. Ceroid lipofuscinosis, neuronal
591. Ceroid lipofuscinosis, neuronal 1, infantile
592. Ceroid lipofuscinosis, neuronal 10
593. Ceroid lipofuscinosis, neuronal 3, Juvenile
594. Ceroid lipofuscinosis, neuronal 4
595. Ceroid lipofuscinosis, neuronal 5
596. Ceroid lipofuscinosis, neuronal 6, late infantile
597. Ceroid lipofuscinosis, neuronal 7
598. Ceroid lipofuscinosis, neuronal 8
599. Ceroid lipofuscinosis, neuronal 9
600. Chagas disease
601. Charcot-Marie-Tooth Disorder
602. Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
603. Charcot-Marie-Tooth disease, Type 4F
604. Charcot-Marie-Tooth disease, type 1
605. Charcot-Marie-Tooth disease, type 2
606. Chemical pneumonia
607. Chest Cold
608. Chiari Malformation
609. Chickenpox
610. Chikungunya
611. Chilblain
612. Childhood hypophosphatasia
613. Childhood liver cancer, primary
614. Childhood-onset cerebral X-linked adrenoleukodystrophy
615. Chitayat-Moore-Del Bigio syndrome
616. Cholera
617. Cholestasis
618. Cholestasis, progressive familial intrahepatic 2
619. Cholestasis, progressive familial intrahepatic 3
620. Cholestatic jaundice -renal tubular insufficiency
621. Chondroblastoma (benign)
622. Chorea
623. Chorea familial benign
624. Chorea, remitting with nystagmus and cataracts
625. Choreoacanthocytosis amyotrophic
626. Choreoathetosis-spasticity, episodic
627. Choroid Plexus neoplasms
628. Choroido cerebral calcification syndrome infantile form
629. Chromosome 1, 1p36 deletion syndrome
630. Chromosome 1, monosomy 1p32
631. Chromosome 1, monosomy 1q25 q32
632. Chromosome 1, monosomy 1q4
633. Chromosome 10p deletion syndrome
634. Chromosome 10p duplication syndrome
635. Chromosome 10p duplication/10q deletion syndrome
636. Chromosome 11q duplication syndrome
637. Chromosome 11q partial deletion
638. Chromosome 12p deletion syndrome
639. Chromosome 12p duplication syndrome
640. Chromosome 12p tetrasomy syndrome
641. Chromosome 12q duplication syndrome
642. Chromosome 13 trisomy syndrome
643. Chromosome 13q deletion syndrome
644. Chromosome 13q duplication syndrome
645. Chromosome 13q partial deletion
646. Chromosome 14 Ring
647. Chromosome 14q deletion syndrome
648. Chromosome 14q, partial deletion
649. Chromosome 14q, terminal deletion
650. Chromosome 15 Ring
651. Chromosome 15 inverted duplication
652. Chromosome 15 trisomy
653. Chromosome 15, trisomy mosaicism
654. Chromosome 15q duplication syndrome
655. Chromosome 15q triplication syndrome
656. Chromosome 15q, partial duplication (distal q arm)
657. Chromosome 15q, partial duplication (unbalanced translocation)
658. Chromosome 15q13.3 microdeletion syndrome
659. Chromosome 16q, partial deletion
660. Chromosome 17 ring
661. Chromosome 17 trisomy mosaicism
662. Chromosome 17, deletion 17q23 q24
663. Chromosome 17p, partial deletion
664. Chromosome 17p, partial duplication
665. Chromosome 17q, partial duplication
666. Chromosome 18 Ring
667. Chromosome 18 deletion syndrome
668. Chromosome 18, trisomy 18q
669. Chromosome 18q, partial deletion
670. Chromosome 19p duplication syndrome
671. Chromosome 19q, partial duplication
672. Chromosome 1p deletion syndrome
673. Chromosome 1p duplication syndrome
674. Chromosome 2 trisomy syndrome
675. Chromosome 2, monosomy 2p22
676. Chromosome 2, monosomy 2pter p24
677. Chromosome 2, monosomy 2q37
678. Chromosome 20p deletion syndrome
679. Chromosome 20p, partial duplication
680. Chromosome 20q duplication syndrome
681. Chromosome 21 monosomy
682. Chromosome 21, tetrasomy 21q
683. Chromosome 21q deletion syndrome
684. Chromosome 22 Ring
685. Chromosome 22, microdeletion 22q11
686. Chromosome 22, monosomy mosaic
687. Chromosome 22, trisomy
688. Chromosome 22q deletion
689. Chromosome 22q deletion syndrome
690. Chromosome 22q duplication syndrome
691. Chromosome 22q11 deletion
692. Chromosome 22q11.2 deletion syndrome
693. Chromosome 22q13 deletion
694. Chromosome 22q13.3 deletion syndrome
695. Chromosome 2p duplication syndrome
696. Chromosome 2q duplication syndrome
697. Chromosome 3, monosomy 3p
698. Chromosome 3, monosomy 3q13
699. Chromosome 3, trisomy 3p
700. Chromosome 3, trisomy 3q
701. Chromosome 4 ring syndrome
702. Chromosome 4, Monosomy 4q
703. Chromosome 4, monosomy 4p14 p16
704. Chromosome 4, trisomy 4p
705. Chromosome 4p deletion syndrome
706. Chromosome 4p15-16 deletion syndrome
707. Chromosome 4q duplication syndrome
708. Chromosome 5, trisomy 5pter p13 3
709. Chromosome 5p duplication syndrome
710. Chromosome 5p tetrasomy syndrome
711. Chromosome 5q duplication syndrome
712. Chromosome 6, monosomy 6p23
713. Chromosome 6p deletion syndrome
714. Chromosome 6q deletion syndrome
715. Chromosome 6q duplication syndrome
716. Chromosome 7, monosomy 7q21
717. Chromosome 7, monosomy 7q3
718. Chromosome 7p duplication syndrome
719. Chromosome 7q duplication syndrome
720. Chromosome 7q partial deletion
721. Chromosome 8 recombinant syndrome
722. Chromosome 8p inverted duplication syndrome
723. Chromosome 8p mosaic tetrasomy
724. Chromosome 8q deletion syndrome
725. Chromosome 8q duplication syndrome
726. Chromosome 9, monosomy 9p
727. Chromosome 9, trisomy 9q32
728. Chromosome 9p tetrasomy syndrome
729. Chromosome 9q deletion syndrome
730. Chromosome 9q duplication syndrome
731. Chromosome 9q duplication/chromosome 9p deletion syndrome
732. Chromosome diploid-triploid mosaicism syndrome
733. Chronic Fatigue Syndrome
734. Chronic Granulomatous Disease
735. Chronic Hepatitis C
736. Chronic Inflammatory Demyelinating Polyneuropathy
737. Chronic Kidney Disease
738. Chronic Myeloproliferative Disorders
739. Chronic adult T-Cell leukemia
740. Chronic berylliosis
741. Chronic myelogenous leukemia
742. Chronic myelomonocytic leukemia
743. Chronic vitamin A toxicity
744. Chylomicron retention disease with Marinesco-Sjogren syndrome
745. Ciguatera poisoning
746. Ciliary dyskinesia-bronchiectasis
747. Cirrhosis of the liver
748. Cirrhosis, familial
749. Citrullinemia I
750. Citrullinemia II
751. Classic childhood ALD
752. Classic galactosemia
753. Cleft lip palate pituitary deficiency
754. Cleft palate
755. Clostridium perfringens food poisoning
756. Clostridium sordellii
757. Coats Disease
758. Cocaine abuse
759. Cocaine withdrawal
760. Coccidioidomycosis
761. Cockayne syndrome
762. Cockayne syndrome type 1
763. Codeine withdrawal
764. Coenzyme Q 10 (CoQ10), deficiency
765. Coenzyme Q cytochrome c reductase deficiency of
766. Coffin-Lowry syndrome
767. Coffin-Siris Syndrome
768. Cogan's syndrome
769. Cohen Syndrome
770. Colchicine toxicity
771. Cold antibody hemolytic anemia
772. Cold contact urticaria
773. Collagenous Colitis
774. Coloboma porencephaly hydronephrosis
775. Colonic Inertia
776. Colonic malakoplakia
777. Colorectal Polyps
778. Colorectal cancer
779. Colpocephaly
780. Combarros Calleja Leno syndrome
781. Combat stress reaction
782. Combined oxidative phosphorylation deficiency 5
783. Common Variable Immunodeficiency
784. Common migraine
785. Complete atrioventricular canal
786. Complex 1 mitochondrial respiratory chain deficiency
787. Complex 2 mitochondrial respiratory chain deficiency
788. Complex 4 mitochondrial respiratory chain deficiency
789. Complex 4 mitochondrial respiratory chain deficiency, benign infantile myopathy
790. Complex 4 mitochondrial respiratory chain deficiency, fatal infant myopathy type
791. Complex 5 mitochondrial respiratory chain deficiency
792. Congenital Muscular Dystrophy
793. Congenital Toxoplasmosis
794. Congenital adrenal hyperplasia
795. Congenital benign spinal muscular atrophy dominant
796. Congenital chloride diarrhea
797. Congenital cystic eye, multiple ocular and intracranial anomalies
798. Congenital cytomegalovirus
799. Congenital disorder of glycosylation type 1/IIX
800. Congenital disorder of glycosylation type 1A
801. Congenital disorder of glycosylation type 1B
802. Congenital disorder of glycosylation type 1C
803. Congenital disorder of glycosylation type 1D
804. Congenital disorder of glycosylation type 1E
805. Congenital disorder of glycosylation type 1F
806. Congenital disorder of glycosylation type 1G
807. Congenital disorder of glycosylation type 1H
808. Congenital disorder of glycosylation type 1I
809. Congenital disorder of glycosylation type 1J
810. Congenital disorder of glycosylation type 1K
811. Congenital disorder of glycosylation type 1L
812. Congenital disorder of glycosylation type 1M
813. Congenital disorder of glycosylation type 2A
814. Congenital disorder of glycosylation type 2B
815. Congenital disorder of glycosylation type 2C
816. Congenital disorder of glycosylation type 2D
817. Congenital disorder of glycosylation type 2E
818. Congenital disorder of glycosylation type 2G
819. Congenital disorder of glycosylation type IIH
820. Congenital disorder of glycosylation, type In
821. Congenital hepatic porphyria
822. Congenital herpes simplex
823. Congenital hypomyelination neuropathy
824.
