Abnormal dermatoglyphics
Symptom Information:
| Symptom ID: | HPO:0007477 | ||||||
| Synonyms: |
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| Cross references: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Regional abnormality of skin(HPO:0011356) Abnormal dermatoglyphics(HPO:0007477) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermal and epidermal conditions NEC(MedDRA:10012424) Abnormal dermatoglyphics(HPO:0007477) |
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| Database Frequency: | 72 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| AREDYLD syndrome | (Orphanet:1133) |
| Absence of fingerprints - congenital milia | (Orphanet:1658) |
| Achalasia - microcephaly | (Orphanet:929) |
| Acrofacial dysostosis, Catania type | (Orphanet:1786) |
| Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
| Böök syndrome | (Orphanet:1262) |
| Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
| Cenani-Lenz syndrome | (Orphanet:3258) |
| Cerebro-reno-digital syndrome | (Orphanet:1396) |
| Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
| Cooper-Jabs syndrome | (Orphanet:1488) |
| Costello syndrome | (Orphanet:3071) |
| Crossed polysyndactyly | (Orphanet:2935) |
| Cryptomicrotia - brachydactyly - excess fingertip arch | (Orphanet:1547) |
| DERMATOGLYPHICS--HYPOTHENAR RADIAL ARCH | (OMIM:221780) |
| DERMATOGLYPHICS--PALMAR TRIRADIUS d, ABSENCE OF | (OMIM:221760) |
| Deafness - genital anomalies - metacarpal and metatarsal synostosis | (Orphanet:3224) |
| Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
| Dermo-odonto dysplasia | (Orphanet:1660) |
| Distal trisomy 18q | (Orphanet:1716) |
| Epiphyseal dysplasia - hearing loss - dysmorphism | (Orphanet:1825) |
| Extrasystoles - short stature - hyperpigmentation - microcephaly | (Orphanet:1964) |
| Fetal alcohol syndrome | (Orphanet:1915) |
| Fetal hydantoin syndrome | (Orphanet:1912) |
| Hand-foot-genital syndrome | (Orphanet:2438) |
| Heart defect - round face - congenital developmental delay | (Orphanet:1355) |
| Hepatic fibrosis - renal cysts - intellectual deficit | (Orphanet:2031) |
| Hidrotic ectodermal dysplasia, Halal type | (Orphanet:1809) |
| Hypertryptophanemia | (Orphanet:2224) |
| IVIC syndrome | (Orphanet:2307) |
| Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
| Intellectual deficit - hypotonia - skin hyperpigmentation | (Orphanet:3050) |
| Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
| Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
| Intellectual deficit, X-linked, Miles-Carpenter type | (Orphanet:85283) |
| Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
| Kabuki syndrome | (Orphanet:2322) |
| Lethal multiple pterygium syndrome | (Orphanet:33108) |
| Lichstenstein syndrome | (Orphanet:2390) |
| Low birth weight - dwarfism - dysgammaglobulinemia | (Orphanet:2621) |
| MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
| Mononen-Karnes-Senac syndrome | (Orphanet:2565) |
| Monosomy 13q14 | (Orphanet:1587) |
| Monosomy 9p | (Orphanet:261112) |
| Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
| Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
| Noonan syndrome | (Orphanet:648) |
| Orofaciodigital syndrome type 10 | (Orphanet:2756) |
| Otofaciocervical syndrome | (Orphanet:2792) |
| Poland syndrome | (Orphanet:2911) |
| Postaxial acrofacial dysostosis | (Orphanet:246) |
| Progeroid syndrome, Petty type | (Orphanet:2963) |
| Qazi-Markouizos syndrome | (Orphanet:3010) |
| Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema | (Orphanet:2252) |
| Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
| Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
| Smith-Lemli-Opitz syndrome | (Orphanet:818) |
| Symphalangism with multiple anomalies of hands and feet | (Orphanet:3246) |
| Synostosis - microcephaly - scoliosis | (Orphanet:3268) |
| Teebi-Shaltout syndrome | (Orphanet:3291) |
| Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
| Thoraco-abdominal enteric duplication | (Orphanet:1759) |
| Toluene embryopathy | (Orphanet:1920) |
| Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
| Trigonocephaly - broad thumbs | (Orphanet:3365) |
| Trisomy 13 | (Orphanet:3378) |
| Trisomy 18 | (Orphanet:3380) |
| Trisomy 9p | (Orphanet:236) |
| Turner syndrome | (Orphanet:881) |
| Williams syndrome | (Orphanet:904) |
| Zlotogora-Ogur syndrome | (Orphanet:3253) |
| Zunich-Kaye syndrome | (Orphanet:3474) |