Curly hair
Symptom Information:
Symptom ID: | HPO:0002212 | ||
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 hair(HPO:0001595) Abnormality of hair texture(HPO:0010719) Curly hair(HPO:0002212) MedDRA: |
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Database Frequency: | 21 / 7739 | ||
Resource: |
All diseases associated with this symptom:
CARDIOFACIOCUTANEOUS SYNDROME 2 | (OMIM:615278) |
CARDIOFACIOCUTANEOUS SYNDROME 3 | (OMIM:615279) |
CHANDS | (OMIM:214350) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cataract - aberrant oral frenula - growth delay | (Orphanet:1373) |
Costello syndrome | (Orphanet:3071) |
Familial benign copper deficiency | (Orphanet:1551) |
Giant axonal neuropathy | (Orphanet:643) |
HAIR MORPHOLOGY 2 | (OMIM:139450) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 | (OMIM:602400) |
Ichthyosis-hypotrichosis syndrome | (Orphanet:91132) |
LEOPARD SYNDROME 2 | (OMIM:611554) |
LEOPARD SYNDROME 3 | (OMIM:613707) |
NOONAN SYNDROME 4 | (OMIM:610733) |
NOONAN SYNDROME 6 | (OMIM:613224) |
NOONAN SYNDROME 8 | (OMIM:615355) |
Naxos disease | (Orphanet:34217) |
Noonan syndrome | (Orphanet:648) |
ONYCHOTRICHODYSPLASIA AND NEUTROPENIA | (OMIM:258360) |
Syndromic diarrhea | (Orphanet:84064) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |