Small nail
Symptom Information:
Symptom ID: | HPO:0001792 | |||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||
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 skin adnexa(HPO:0011138) Abnormality of the nail(HPO:0001597) Aplasia/Hypoplasia of the nails(HPO:0008386) Small nail(HPO:0001792) MedDRA: |
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Database Frequency: | 55 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
ADAMS-OLIVER SYNDROME 1 | (OMIM:100300) |
ADAMS-OLIVER SYNDROME 2 | (OMIM:614219) |
ALG3-CDG | (Orphanet:79321) |
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib | (OMIM:615631) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Adams-Oliver syndrome | (Orphanet:974) |
BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION | (OMIM:613627) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
Cutis gyrata - acanthosis nigricans - craniosynostosis | (Orphanet:1555) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
Deafness - onychodystrophy | (Orphanet:3231) |
Deafness - onychodystrophy, autosomal dominant | (Orphanet:79499) |
Distal monosomy 10q | (Orphanet:96148) |
Distal symphalangism | (Orphanet:3248) |
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY | (OMIM:614520) |
Ectodermal dysplasia - syndactyly syndrome | (Orphanet:247820) |
FACIOTHORACOGENITAL SYNDROME | (OMIM:227320) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Familial clubfoot due to 17q23.1q23.2 microduplication | (Orphanet:238578) |
Fibular aplasia - complex brachydactyly | (Orphanet:2639) |
Fryns syndrome | (Orphanet:2059) |
GELEOPHYSIC DYSPLASIA 1 | (OMIM:231050) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Geleophysic dysplasia | (Orphanet:2623) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hirschsprung disease - nail hypoplasia - dysmorphism | (Orphanet:2153) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Hypodontia - dysplasia of nails | (Orphanet:2228) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 | (OMIM:242100) |
Lethal polymalformative syndrome, Boissel type | (Orphanet:210144) |
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT | (OMIM:608257) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Palmoplantar keratoderma-sclerodactyly syndrome | (Orphanet:384) |
Polysyndactyly - cardiac malformation | (Orphanet:2934) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH | (OMIM:606895) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Self-healing collodion baby | (Orphanet:281122) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Sotos syndrome | (Orphanet:821) |
TRICHORRHEXIS NODOSA SYNDROME | (OMIM:275550) |
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 | (OMIM:234050) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Williams syndrome | (Orphanet:904) |
Zechi-Ceide syndrome | (Orphanet:217017) |
Zimmermann-Laband syndrome | (Orphanet:3473) |